M.E/chronic fatigue syndrome

[AwakeningtoMe]

Well finally someone who understands what it feels like to have Chronic Fatigue. It annoys me when people say I'm lazy when I've accomplished so much in my life..but it's sad that i've had to suffer from it really bad in the last 3 years to the pain and watch everyone I love turn their back on me. It's been hard because I've had it around 17 years, since i was around 16 (or maybe before it..but that's when the doctor first identified it). But Thank you!

[HarleyQuinn2513]

Have had CFS since last year today! Feel depressed and just want to be my old self again. CFS has even effected my appearance and confidence. At school I feel even for paranoid and I just want to never go to school and curl up in a hole and cry! Thank You for this video it makes me understand I'm nit alone however! Thank You. xx

[lillibug28]

I've had M.E for about a year now. I had to leave my A levels and like the majority of others with M.E, spent the virtually all of my year in clinic or hospital. I'm still not better, but I'm back to school for one lesson, and ever time I go, it kills me. Its caused me to become depressed and I have always been a happy positive person, despite anything thats happend. It's amazing how many people tell me to "man up" everyday

I guess all we can do is just stick in there and hope for the best. Hugs

[Marc301257]

Hai,

Here is a big HUG from me! I have it to and not one day is the same,.

I lost my job and so on.

[ChibiYotsuba]

By the way... that worktraining is in another town. How am I to get there, if moving through the house is difficult?

[ChibiYotsuba]

A jobcoach actually told me today that, even if I feel like I can even barely move through the house, I should still try to come to the worktraining. She doesn't want to allow me to call in sick then. She believes that I can overcome this by just moving my boundries by simply doing it, even if that puts me in risk of a hyperventilation attack. This jobcoach is supposed to help people with psychological and bodily disfunctions getting a job.

I got so frustrated today!

[nz804]

One lady said to me "Harden Up" and she said it looking upset and angry at me. Far out the amount of crap I have had from people who don't understand. Oh you just have depression they would say to me, you are just lacking in vitamins take a B vitamin and you will be all better they say to me, not a damn clue what they are talking about, they think everything can be fixed easy and that I can do things like run like everybody else. Human beings can be very cold!

[nz804]

I have had M.E for 1 year and 1 month now it is horrible you can only do things for so long before you get wiped out with fatigue. I was on a medication that made me throw up for 3 months. It destroyed my immune system and I now have M.E. I am only 22 years old and my life has just begun, I can pretty much throw it all down the drain now, I am screwed.

[mellbutler]

my heart aches, this video sums it all up....those days stuck inside yourself looking out from the inside, inside ourselves and inside our homes. for the past 8 years i have suffered alone.....but thankful I am somewhat functional and finndling my own way into feeling better

[nancypittman]

I love this video! Only cfs sufferers can really understand it !

[KellyOldershaw]

Great video. Recovery is absolutely possible and having recovered myself, I want to offer hope to others. please come and access your free healing meditation for me, cfs & fibromyalgia and the 13 1/2 essentials to recovery at getyourlifebackfromme. com

[ShadowxMaker]

You know the only thing that keeps me moving is skateboarding. I try do it almost every day and it takes a lot of effort and energy but once I get moving I'm alert and in more control but once I stop and sit down.... All hell breaks loose...

[systemawarrior]

Keep your chin up. I wish you all the best of health. Have faith in your bodies healing ability and provide it with the nutrition it needs to do the healing.

It will take time and sometimes its 1 step forward and 2 steps back .

Keep well.

[trumarksurfnut]

This is so good. Not sure how many people I know who dont have it would stick with it till the end, but great work! Keep it up :) Bri

[IxLIKExURxVIDx]

If any honest sufferer has any treatment or anything that helped them on the path back to recovery, please respond to this message as i am soooo confused how to try to get better???? :(

[alexsantoro]

@IxLIKExURxVIDx ,

It is my belief that you can heal ME/CFS with nutrition and lifestyle.

Do a search for: ME (Myalgic Encephalomyelitis) and CFS (Chronic Fatigue Syndrome). There IS a cure - Day 1 of 200 , and watch some of my videos. I am on Day 12 and already feel hardly any symptoms.

Eventhough a lot of people are saying that I am giving people "false hope", I know I can prove that we can heal ourselves and I can help you. Keep watching my journey and I will prove it to you.

[IxLIKExURxVIDx]

This video really does sum everything up. I also posted this on facebook, as there are many people how know very little of this terrible illness. Everyone with ME/CFS stay strong. xx

[GetFitt1]

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[tweety932]

Thank you for this video. It says so much about a misunderstood disease. I've lost so much to this disease, the person I use to be, the ability to work, my marriage, my memory, etc. I don't want pity from anyone just empathy. But it's hard for anyone who doesn't have the disease to understand. When I'm with other people I try to be upbeat and hide what I'm going thru because no one wants to be around a downer. But then I'm accused of having "selective energy" or being lazy (I loved your poster).

[Ashapa1]

For all the skeptics : THIS THING IS REAL !!!!

I wish all the sufferers a relief , a recovery , a cure , and finally a comeback of their previous lives !!

[Ashapa1]

Meggy , this video was so heart-rending . You , and the people who suffer this horrible disease mustn't apologize for anything !! You already live with terrible guilt feelings , and have to deal with such a paralyzing illness , not on a daily basis, but on a minute basis !! And I know , because I had suffered from CFS for 7 years , and had just cured not long ago. I truly care about the sufferers, who are castaway in an endless battle, so alone.. with a drop of energy.. I WISH YOU WELL !!!!!

[brisbanette]

Cried through most of it - very powerful. If people had these illnesses (ME or CFS or FM) for even just a week they might actually understand how bad it really is.

[shazaonator]

Thank you for sharing your story, it has been 7 years for me now, better than at the start but still suffering, posted this on my facebook profile, what you said sums me up quite a lot too, if there was a cure I would be in line waiting for it. Get Well Soon. We all deserve to get ourselves back.

[LSecret]

I'm posting this on my Facebook and sending it to my colleagues.

I apreciate your posting this video.

I know how you feel (-_-)

[mellraizer]

wow. that pretty much summed it up. like nothing else.

it is possible to get better... a awfull & incredibly long experience nevertheless.. but i hope to get there along with everyone else.

thanks, i hope this helps understanding on all fronts : ))

[hosslady]

Thank you ♥ I also have this horrible illness and have lost my previous life because of it. Because I mostly look OK people think it's all in your head and we know it's not! I was actually relieved when my white cell count came back really low because it proved it was REAL.

[Applechewbacca]

Whoa, this really sums up me quite a lot. Hope you feel better. x

[Claggy]

Very good video. I am currently at the beginning of my recovery from CFS/ME after 5 years, and will soon have my life back! Thank you for helping spread awareness!

[3DeeFanatic]

@Claggy how are you recovering ?? i need to get out of it !

[Claggy]

It is a long process, but I'm on the right path. I'm currently a part of the nutrition and psychology areas of a clinic. I highly suggest checking out this link and reading around, watching videos, getting the free info packet, and just whatever you can do to. Just remove the spaces and () from it. freedomfromme (.) co (.) uk/

[freedomfromme]

Thanks for this moving video. Please do have a look at the specialised videos on our channel concerning chronic fatigue syndrome

[bundybearable]

Oh god.. Loneliness isn't the word..

[kaybaron1]

I watched this video with tears streaming down my face xx

[alittlepintail]

I take Morphine to be able to now function at any level because of the pain. My brain is mush, I could do a high level job, now i even forget to sign my own name. I was sporty, now i cant complete everyday tasks. I lost my marriage and feel no one will ever put up with my illness what do i have to offer anyone. My children dont understand they think im just lazy. Freinds try but cant comprehend you can look so well yet feel so ill. I cried when i saw this as it said it all x

[augustbabe1964]

oh honey i feel for you so much & completely understand how you feel. contact me anytime via my mail box - even if its just a moan it does help to share and know that u are not alone. my me gets worse each month and i sometimes despair but together we may just get there tracyx

[cpettet]

i have had cfs for 9 months now and this video speaks so many feelings and thoughts i have never said, i have had alot of trouble with support from the people i most expected it , and coming to terms with the slow and unsure path the future holds, has been my biggest hurdle. But the only thing i have to hold onto is hope, and i do hope that one day i will be able to do all the things that make me who i am. And that one day i wil be able to go back to university and to work.

Thankyou xxx

[Anii100]

thanks for posting this video its great to see supportive videos and such, just raising awareness, ive had M.E for three years now and its so hard trying to explain to people. So thanks alot :)

[augustbabe1964]

Thank you so much for posting this - i am having a bad few days and it really does help to know that there is understanding out there. My hubby keeps saying that he wants the old "me" back but after 3+ years i cant remember who i was back then. I have just lost my job which was my last link with my "good" life and only have my DLA appeal board to look forward too ;-(( big hug xx

[sleepythatsnotall]

iv had CFS for about 3 years but i think im finally reaching the end, its a bit scary to say that but im going to school regularly, im walking to the bus, im even doing sport and PE!!!! (all things at one point i feared i might never do again) its a long hard road, and its cliched but im a better person for having this illness. your not alone, there is always help. dont give up, you will get through this

[papageilo1]

thank you for that... thank you...

[papageilo1]

i heard about a medical test that will come in the next years, its a bloodtest wich is checking the activies of some genes in the blood, these genes are 4x higher at CFS patients then on healthy persons

sry for my bad english!

[NikkoYM]

thank you thank you thank you for this "public service announcement"

[FibroMeandCFShope]

Such a wonderful video. I suffer along with you. It helps to know others understand your life.

[zefrongurl4567]

this puts all my feelings in2 words.

thanks, i have had had M.E. 4 4 years so far...

its hard:-(

hope everyone is haveing a gud day with it:-)

love

xoxoxo

[Leharik]

Great video! Well done!

It actually made me cry because I used to have CFS too.

My message is that IT IS possible to get well. I'm in a process of publishing my book online. Hopefully it will help many.

[DrFrankyDolan]

Thank you so much for sharing with us! I am working hard as well to raise awareness and bring our community together.

Great work!

We WILL get better my friends, we will...

Sending love.

[LovelyWhiteWitch]

That was a very touching video. I'll put it in my multiply site (CFS/ME awareness).

Love, wellness and joy to you... *hugs*

[bmwrider52]

For those who has ME/ chronic fatigue syndrom: check out eft for chronic fatigue on youtube. this is an easy technic that actually can lead us to a healty state again :)

[peacelovemiffy]

thanks for posting this. i will show it to some friends so they can have a better understanding. i am on a 'good' day today and hope you are too. hugs..x

[SANDMANCASTHISSPELL]

A great Video;-)

Sandman Cast His Spell

[Scizza123]

Watching it again. :)

It really is Vair good. :)

[tweety932]

Thank you for this video. I am trying to put a collection together to share with friends and family to help them understand my illness. I love the whole thing you did a wonder job but I love the signs towards the ends. I will have to remember to tell myself that - I am not lazy it is a relapse and I am in pain because I am in pain. That gives light to the darkness of this illness. Thanks again.

[finette4444]

Thank-you so much for a beautiful and moving video. You are lucky if you have family and friends that help and support you - so many don't.

[jessa982]

wow ! :)

its really good ... loved it all . got tears streaming down my face though now !

well done , you put alot into it !

Jess x

[themelii93]

woah that was amazing!

well done that must have taken ages! love you xxx mel

[Scizza123]

wow meg :D

thats on my bebo page now!!

also I really love the apology bit :D :D

well done ! :D

SarahJayne x

[6pop7]

u put a lot off work into that :) from kieran